Validation Engineer

Key Responsibilities:

• Conduct quality investigations with a focus on sterile/aseptic fill processes.
• Execute Commissioning, Qualification, and Validation (CQV) activities, including thermal mapping.
• Manage sterilization and steam-in-place (SIP) processes as needed.
• Maintain on-site presence during core hours, Monday to Friday, 7 AM - 3 PM.

Qualifications:

• 8+ years of experience in quality investigations.
• Demonstrated experience in sterile/aseptic fill CQV and thermal mapping.
• Sterilization/SIP experience is a plus.